Congenital analbuminemia with acute glomerulonephritis: a diagnostic challenge
暂无分享,去创建一个
[1] T. Stallmach,et al. A boy with congenital analbuminemia and steroid-sensitive idiopathic nephrotic syndrome: an experiment of nature , 2008, European Journal of Pediatrics.
[2] G. Caridi,et al. Analbuminemia produced by a novel splicing mutation. , 2007, Clinical chemistry.
[3] M. Galliano,et al. Analbuminemia in a Slovak Romany (gypsy) family: case report and mutational analysis. , 2006, Clinica chimica acta; international journal of clinical chemistry.
[4] Š. Rosipal,et al. A speculation about hypercholesterolemia in congenital analbuminemia. , 2006, The American journal of medicine.
[5] M. Arca,et al. Congenital analbuminemia attributable to compound heterozygosity for novel mutations in the albumin gene. , 2005, Clinical chemistry.
[6] R. Houwen,et al. Congenital analbuminaemia: biochemical and clinical implications. A case report and literature review , 2004, European Journal of Pediatrics.
[7] A. Lyon,et al. Molecular diagnosis of analbuminemia: a novel mutation identified in two Amerindian and two Turkish families. , 2002, Clinical chemistry.
[8] A. Lyon,et al. Influence of methodology on the detection and diagnosis of congenital analbuminemia. , 1998, Clinical chemistry.
[9] M. Galliano,et al. Analbuminemia: three cases resulting from different point mutations in the albumin gene. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[10] B. Brenner,et al. Role for intrarenal mechanisms in the impaired salt excretion of experimental nephrotic syndrome. , 1983, The Journal of clinical investigation.
[11] H. Bennhold,et al. Über einen Fall von kompletter Analbuminaemie ohne wesentliche klinische Krankheitszeichen , 1954 .